Other congenital malformation syndromes predominantly associated with short stature
ICD-10 Q87.19 is a billable code used to indicate a diagnosis of other congenital malformation syndromes predominantly associated with short stature.
Q87.19 encompasses a variety of congenital malformation syndromes that are primarily characterized by short stature, which may be accompanied by other physical anomalies. These syndromes can include a range of congenital malformations affecting various organ systems, including skin, breast, spleen, and adrenal glands. For instance, conditions such as Turner syndrome, which is associated with short stature and various physical anomalies, may fall under this code. Other syndromes may present with unique combinations of malformations, such as congenital skin lesions, breast hypoplasia, or splenic agenesis. The complexity of these syndromes often requires a multidisciplinary approach for diagnosis and management, involving pediatricians, geneticists, and other specialists. Accurate coding is essential for appropriate treatment planning and resource allocation, as well as for research and epidemiological tracking of these rare conditions.
Pediatric documentation should include growth charts, detailed physical examination findings, and any associated congenital anomalies.
Common scenarios include evaluation of short stature in children with known congenital syndromes, and management of associated complications.
Pediatric coders must ensure that all congenital anomalies are documented and linked to the primary diagnosis.
Genetic documentation should include family history, results of genetic testing, and any syndromic features observed.
Genetic counseling for families with a history of congenital malformations and the diagnosis of syndromes through genetic testing.
Genetic coders must be aware of the specific genetic markers associated with various syndromes to ensure accurate coding.
Used when evaluating a patient for Turner syndrome due to short stature.
Documentation of clinical findings and rationale for genetic testing.
Geneticists should ensure that the testing aligns with the clinical presentation.
Q87.19 includes a variety of congenital malformation syndromes that are predominantly associated with short stature, such as Turner syndrome and other syndromes with unique combinations of congenital anomalies affecting skin, breast, spleen, and adrenal glands.
